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Merck

498041

Sigma-Aldrich

环戊基溴化锌 溶液

0.5 M in THF

别名:

Bromo(cyclopentyl)zinc, Bromocyclopentylzinc

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About This Item

线性分子式:
C5H9ZnBr
分子量:
214.42
MDL號碼:
分類程式碼代碼:
12352103
PubChem物質ID:
NACRES:
NA.22

濃度

0.5 M in THF

密度

0.955 g/mL at 25 °C

儲存溫度

2-8°C

SMILES 字串

Br[Zn]C1CCCC1

InChI

1S/C5H9.BrH.Zn/c1-2-4-5-3-1;;/h1H,2-5H2;1H;/q;;+1/p-1

InChI 密鑰

GOPYCBPMCCJYSN-UHFFFAOYSA-M

應用

Cyclopentylzinc bromide is an organozinc reagent that can be used in:
  • The synthesis of polyfunctional indoles by reacting with various aryldiazonium salts via Fischer indole synthesis.
  • Negishi cross-coupling reactions with various haloarenes in presence of Pd-complex catalyst.
  • The preparation of aryl alkyl ketones by alkylation of aryl N-methyl-N-tosyl or N-benzyl-N-(tert-butoxycarbonyl) amide derivatives in the presence of Ni catalyst and imidazolidinylidene ligand.

法律資訊

Rieke® Metals, Inc. 制造。®Rieke Metals, Inc. 的注册商标。

訊號詞

Danger

危險分類

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3 - Water-react 2

標靶器官

Respiratory system

安全危害

儲存類別代碼

4.3 - Hazardous materials which set free flammable gases upon contact with water

水污染物質分類(WGK)

WGK 3

閃點(°F)

1.4 °F - closed cup

閃點(°C)

-17 °C - closed cup


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分析证书(COA)

Lot/Batch Number

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访问文档库

Mild Negishi cross-coupling reactions catalyzed by acenaphthoimidazolylidene palladium complexes at low catalyst loadings
Liu Z, et al.
The Journal of Organic Chemistry, 78(15), 7436-7444 (2013)
Efficient preparation of polyfunctional indoles via a zinc organometallic variation of the Fischer indole synthesis
Zhang Z-G, et al.
Synthesis, 2011(01), 23-29 (2011)
Nickel-catalyzed alkylation of amide derivatives
Simmons BJ, et al.
ACS Catalysis, 6(5), 3176-3179 (2016)

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